亚稳态
纳米颗粒
催化作用
材料科学
化学物理
解吸
化学工程
金属
分子
纳米技术
化学
物理化学
吸附
冶金
有机化学
工程类
作者
Samantha L. Le,C. R. O'Connor,Taek‐Seung Kim,C. Reece
标识
DOI:10.1002/anie.202423880
摘要
The dynamic response of heterogeneous catalytic materials to their environment opens a wide variety of possible surface states which may have increased catalytic activity. In this work, we find that it is possible to generate a surface state with increased catalytic activity over metallic 2nm Pt nanoparticles by performing a thermal treatment of the CO*‐covered Pt catalyst. This state is characterised by its ability to oxidise CO to CO2 at room temperature. By combining pressure pulse experiments with in situ spectroscopy we correlate the formation of this high‐activity state with the desorption of weakly bound CO* molecules from well‐coordinated Pt sites. This high‐activity state is metastable, degrading after elevated thermal treatments or upon readsorption of CO at room temperature. We conclude that this metastable state is highly localised to the surface of the nanoparticle, however its exact atomic structure remains open to speculation.
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